Fast ion conductors
United States Patent 5352544

In units comprising solid polymer electrolytes, the ionic conductivity of such electrolytes is increased by mechanically exciting the units. Such units can be solid state batteries or electrochromic devices or the like. Mechanical excitation may be provided by, for example, a piezoelectric transducer.

Kumar, Binod (Centerville, OH)
Marsh, Richard A. (Tipp City, OH)
Application Number:
Publication Date:
Filing Date:
The United States of America as represented by the Secretary of the Air (Washington, DC)
Primary Class:
Other Classes:
429/307, 429/312
International Classes:
H01M10/052; H01M10/0565; H01M10/42; G02F1/15; (IPC1-7): H01M14/00
Field of Search:
429/4, 429/7, 429/192
View Patent Images:
US Patent References:
5162175Cell for making secondary batteries1992-11-10Visco et al.429/192
5061581Novel solid polymer electrolytes1991-10-29Narand et al.429/192
4888257Solid electrolyte1989-12-19Narang429/192
4886716Solid polymeric electrolyte and electrochemical generators containing it1989-12-12Roggero et al.429/192
4826743Solid-state lithium battery1989-05-02Nazri429/191
4025698Accumulator battery apparatus and method1977-05-24von Krusenstierna429/4

Primary Examiner:
Kalafut, Stephen
Attorney, Agent or Firm:
Bricker, Charles E.
Kundert, Thomas L.
We claim:

1. A method for increasing the ionic conductivity of the solid polymer electrolyte in a unit consisting essentially of an electrode, a counter-electrode, a solid polymer electrolyte between said electrode and said counter-electrode, a first electrical contact in conducting relation with said electrode, a second electrical contact in conducting relation with said counter-electrode, and a housing holding said electrical contacts, said electrode, said counter-electrode and said polymer electrolyte, which comprises mechanically exciting said unit.

2. The method of claim 1 wherein said mechanical excitation is provided by piezoelectric means.

3. The method of claim 1 wherein said excitation is provided in the frequency range of 40 to 400 KHz.

4. The method of claim 1 wherein said unit is a solid state battery.

5. The method of claim 4 wherein said battery is a lithium cell.

6. The method of claim 1 wherein said unit is an electrochromic device.

7. A solid state battery system which comprises a solid state battery having a solid polymer electrolyte and means for mechanically exciting the polymer electrode, wherein said excitation means is in physical contact with said battery.

8. The battery system of claim 7 wherein said solid state battery is a lithium cell.

9. The battery system of claim 8 wherein said polymer electrolyte is polyethylene oxide doped with LiClO4.

10. The battery system of claim 7 wherein said means for mechanically exciting said polymer electrolyte is a piezoelectric transducer.



This invention relates to solid polymer electrolytes useful in rechargeable batteries, power supplies, capacitors and microelectrochemical sensors.

Lithium has long been regarded as a desirable component of galvanic cells. It is inexpensive and its high reduction potential (E°red =-3.024 v) and light weight have often suggested its use as the anodic component in high energy-density storage batteries. The reactivity of Li with water has required the use of non-aqueous electrolytes such as organic soluble lithium perchlorates, or fused lithium halides. Li+ conductors which are solid and are more highly conductive at lower temperatures than previously used electrolytes would be quite useful in such utilities; these conductors also serve to separate the anodic and cathodic components.

Solid electrolytes and in particular completely solid state galvanic cells offer special advantages as high-energy density, high-power density primary batteries. These advantages include the possibility for long shelf life, broad temperature limits of operability and miniaturization. A Li+ conducting solid electrolyte would provide the basis for a lighter and lower cost alternative to the solid state batteries which rely in the transport of Ag+ in various silver halides.

Solid electrolytes for use in batteries and other electrochemical devices must have good ionic conductivity in addition to excellent film forming properties and good storage stability. Moreover, the solid electrolyte must be simple to produce.

It is known that inorganic solid electrolytes such as Na--β--Al2 O3 and Na1+x Zr2 P3-x Six O13 (where x is 0 to 3) have good ionic conductivity. However, these inorganic solid electrolytes have very low mechanical strength and are difficult to process into a flexible film.

Further, it is known that complexes of certain polymeric materials and various salts of metals belonging to Group I or Group II of the Periodic Table (e.g., LiCF3 SO3, LiI, LiB, LiClO4, NaI, NaCF3 SO3 and KCF3 SO3) function as solid electrolytes. These polymers include polyethylene oxide (PEO), polypropylene oxide (PPO), poly(ethylene adipate) (PEA), poly(ethylene succinate) (PES), polyphosphazine (PPhz), polysiloxane, poly(N-methylaziridine) (PmAZ), triol type PEO crosslinked with dysfunctional urethane, PEO-PPO-PEO block copolymer crosslinked with trifunctional urethane, and the like. These complexes have good pliability and viscoelasticity, both of which are inherent to polymeric materials, and are easy to process.

High energy density, rechargeable solid polymer electrolyte-using solid state batteries promise virtually maintenance-free reliable operation over many thousands of cycles. However, the ionic conductivity of the above polymers is highly temperature dependent. Although the ionic conductivity is good at temperatures above room temperature, the ionic conductivity abruptly decreases at room temperature or lower. Thus it is difficult to use these polymers in general purpose commercial products for use over a wide temperature range.

Accordingly, it is an object of the present invention to provide a method for increasing the ionic conductivity of solid polymer electrolytes, particularly at and below room temperature.

It is another object of the present invention to provide a solid state battery system exhibiting reliable operation at and below room temperature.

Other objects and advantages of the invention will be apparent to those skilled in the art.


In accordance with the present invention there is provided a method for increasing the ionic conductivity of solid polymer electrolytes which comprises mechanically exciting the units which comprise the polymer electrolytes.

There is also provided a solid state battery system which comprises a solid state battery having a solid polymer electrolyte and means for mechanically exciting the polymer electrolyte.


In the drawings:

FIG. 1 is a sectioned perspective view of a solid-state battery;

FIG. 2 is a graph of resistivity vs temperature for a variety of conductive polymers;

FIG. 3 is a schematic diagram of a solid-state battery in accordance with the invention;

FIG. 4 is a sectioned view of an electrochromic device in accordance with the invention;

FIG. 5 is a graph of discharge rate vs time for a 6 v solid-state battery with a circuit load of 1 K-ohm, with and without excitation; and

FIG. 6 is a graph of discharge rate vs time for a 6 v solid-state battery with a circuit load of 22 K-ohm, with and without excitation.


FIG. 1 illustrates a typical lithium cell wherein a solid polymer electrolyte 1 is sandwiched between a lithium electrode 2 and a counter-electrode 3 (e.g., MnO2) which in turn is sandwiched between two metal electrical contacts 4 and 5, held in a plastic housing 6.

Polymers having reasonably high conductivity, i.e., at least about 10-3 Siemens (S) cm-1, at temperatures about 50°-100° C. are generally considered acceptable for use in solid state batteries. The conductivity of such polymers exhibit strong temperature dependence as shown in FIG. 2. As seen in FIG. 2, LiClO4 -doped PEO is the only electrolyte, among those shown, to achieve this desired conductivity, and then only at temperatures of about 80° C. and above.

The conductivity of solid polymer electrolytes is increased by mechanical excitation. Such excitation may be accomplished by incorporating with or securely attaching a suitable transducing device to the device under consideration. FIG. 3 illustrates a self-primed battery in accordance with the invention which comprises a solid polymer electrolyte-containing solid state battery 10 having a transducer means 12 attached thereto. Battery 10 has contact means 14 and 16 for attachment to primary power leads 18 and 20, which in turn connect to an external load, not shown. Also connected to contact means 14 and 16 are secondary power leads 22 and 24 which provide electrical power to transducer means 12. Power lead 22 includes switching means 26 so that the transducer means can be turned on and off, as necessary. The transducer means 12 comprises appropriate circuitry, not shown, for driving the transducer. Piezoelectric transducers are well suited for this application, although other electro-mechanical transducers may also be used.

The response of electrochromic devices based on WO3 and having a polymer electrolyte can be enhanced by mechanical excitation. FIG. 4 illustrates such a device 30, comprising a lithium-coated first electrode 32, a WO3 -coated second electrode 34 and a polymer electrolyte 36 disposed therebetween. At least one transducer means 38 is attached to device 30 in such manner that excitation produced by transducer means 38 is mechanically coupled to electrolyte 36.

The following example illustrates the invention:


The batteries employed in this example had a rated capacity of 20 mAh with a nominal voltage of 6 v. These batteries are available commercially from Gould Electronics, East Lake, Ohio 44095, under the tradename Thinergy.

The batteries were taped to the bottom of an ultrasonic cleaner for mechanical excitation over a frequency range of 40-400 KHz. The discharge rates were determined under loads of 1 K-ohm and 22 K-ohm at a temperature of about 31°C., with and without mechanical excitation.

Referring to FIG. 5, it can be seen that under a circuit load of 1 K-ohm and without mechanical excitation, the discharge rate of the battery decreases almost linearly over the period 30-120 sec. In contrast, when mechanically excited, at about 40-400 KHz, the discharge rate initially decreases, but begins to increase after about 90 sec.

Referring to FIG. 6, when tested with a 22 K-ohm load and without mechanical excitation, the battery exhibited a similar decrease in discharge rate over time. However, with mechanical excitation, the battery exhibits an increase in discharge rate.

Various modifications may be made to the invention as described without departing from the spirit of the invention or the scope of the appended claims.